CN113185735A - Anti-freezing supramolecular hydrogel electrolyte film and preparation and application thereof - Google Patents
Anti-freezing supramolecular hydrogel electrolyte film and preparation and application thereof Download PDFInfo
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- 239000000017 hydrogel Substances 0.000 title claims abstract description 74
- 239000003792 electrolyte Substances 0.000 title claims abstract description 48
- 238000002360 preparation method Methods 0.000 title claims abstract description 20
- 238000007710 freezing Methods 0.000 title abstract description 17
- 239000000178 monomer Substances 0.000 claims abstract description 30
- 239000007864 aqueous solution Substances 0.000 claims abstract description 21
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- 239000000463 material Substances 0.000 claims abstract description 19
- 239000012266 salt solution Substances 0.000 claims abstract description 8
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 7
- 238000002791 soaking Methods 0.000 claims abstract description 3
- 239000000243 solution Substances 0.000 claims description 21
- 230000002528 anti-freeze Effects 0.000 claims description 19
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 13
- -1 3- (methacrylamido) propyl Chemical group 0.000 claims description 11
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 11
- 239000000908 ammonium hydroxide Substances 0.000 claims description 11
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 238000003756 stirring Methods 0.000 claims description 10
- 239000011521 glass Substances 0.000 claims description 8
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 claims description 6
- 239000012528 membrane Substances 0.000 claims description 6
- 238000005303 weighing Methods 0.000 claims description 5
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- 239000008367 deionised water Substances 0.000 claims description 4
- 229910021641 deionized water Inorganic materials 0.000 claims description 4
- 239000003999 initiator Substances 0.000 claims description 4
- 229920001467 poly(styrenesulfonates) Polymers 0.000 claims description 3
- 229960002796 polystyrene sulfonate Drugs 0.000 claims description 3
- 239000011970 polystyrene sulfonate Substances 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- GKWLILHTTGWKLQ-UHFFFAOYSA-N 2,3-dihydrothieno[3,4-b][1,4]dioxine Chemical compound O1CCOC2=CSC=C21 GKWLILHTTGWKLQ-UHFFFAOYSA-N 0.000 claims description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 2
- INHCSSUBVCNVSK-UHFFFAOYSA-L lithium sulfate Inorganic materials [Li+].[Li+].[O-]S([O-])(=O)=O INHCSSUBVCNVSK-UHFFFAOYSA-L 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- 239000001103 potassium chloride Substances 0.000 claims description 2
- 235000011164 potassium chloride Nutrition 0.000 claims description 2
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 claims description 2
- 229910052939 potassium sulfate Inorganic materials 0.000 claims description 2
- 235000011151 potassium sulphates Nutrition 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 2
- 235000011152 sodium sulphate Nutrition 0.000 claims description 2
- RBTVSNLYYIMMKS-UHFFFAOYSA-N tert-butyl 3-aminoazetidine-1-carboxylate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)N1CC(N)C1 RBTVSNLYYIMMKS-UHFFFAOYSA-N 0.000 claims description 2
- 108010053481 Antifreeze Proteins Proteins 0.000 claims 2
- 230000008014 freezing Effects 0.000 abstract description 6
- 239000007785 strong electrolyte Substances 0.000 abstract description 2
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- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 6
- 239000003990 capacitor Substances 0.000 description 6
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- 229920000642 polymer Polymers 0.000 description 4
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- 150000002500 ions Chemical class 0.000 description 3
- 229920002125 Sokalan® Polymers 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 238000000113 differential scanning calorimetry Methods 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
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- 239000004584 polyacrylic acid Substances 0.000 description 2
- BCAIDFOKQCVACE-UHFFFAOYSA-N 3-[dimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azaniumyl]propane-1-sulfonate Chemical compound CC(=C)C(=O)OCC[N+](C)(C)CCCS([O-])(=O)=O BCAIDFOKQCVACE-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 1
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- 230000005540 biological transmission Effects 0.000 description 1
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- 238000010277 constant-current charging Methods 0.000 description 1
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- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 239000002001 electrolyte material Substances 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000021715 photosynthesis, light harvesting Effects 0.000 description 1
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- 239000007784 solid electrolyte Substances 0.000 description 1
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
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- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
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Abstract
The invention discloses a freezing-resistant supramolecular hydrogel electrolyte film and preparation and application thereof, wherein the supramolecular hydrogel electrolyte film is prepared by a two-step synthesis method, and is prepared by firstly mixing two monomers of PDP and AA in water, ensuring the molar ratio of PDP to water molecule to be 1:6, obtaining pre-prepared supramolecular hydrogel through polymerization reaction, and then soaking the supramolecular hydrogel electrolyte film in a strong electrolyte salt solution. The prepared electrolyte film material has excellent frost resistance by strictly controlling the molar ratio of the monomer to the aqueous solution, can normally work in a wider temperature range, and has wide application prospect in the field of flexible and stretchable electronic devices.
Description
Technical Field
The invention belongs to the technical field of high-molecular photoelectric materials, and particularly relates to an antifreeze supramolecular hydrogel electrolyte film and preparation and application thereof.
Background
With the popularization and development of 5G networks and intelligent terminals, wearable electronic equipment with the flexible and stretchable characteristics shows huge market application prospects. Currently, wearable electronics are used in many aspects of human life, such as flexible energy storage devices, wearable physiological detection devices, and the like. Flexible stretchable electronic devices are generally assembled from flexible electrolytes and flexible electrodes in a "sandwich" structure, and hydrogel-based electrolyte materials are widely used and studied in the field of flexible solid electrolytes because of their good flexibility and ionic conductivity. Meanwhile, the hydrogel has good biocompatibility and can coexist with human tissues, so that good wearability is realized.
Hydrogel-based ionic devices are capable of converting an external stimulus into an electrical signal. However, in practical applications, once the temperature drops below the freezing point of water, the hydrogel freezes, limiting its temperature range of use. Therefore, there remains a significant challenge to develop ion devices that can maintain their performance in extreme environments. And the traditional hydrogel has the problems of single and uneven network structure, lack of energy dissipation mechanism and the like, so that the mechanical strength is limited and the traditional hydrogel has a large gap with natural tissues.
In view of the above problems, those skilled in the art have made corresponding improvements, for example, chinese patent CN 110265232 a discloses a self-healing hydrogel electrolyte membrane, and a preparation method and an application thereof, the electrolyte membrane is prepared by copolymerizing [2- (methacryloyloxy) ethyl ] dimethyl- (3-sulfopropyl) ammonium hydroxide and methacrylic acid monomers, and a polymer network inside the gel electrolyte is crosslinked by means of reversible non-covalent bonds such as hydrogen bonds, so that the gel electrolyte membrane has the characteristics of being overstretched, self-healing and the like. The mechanical property of the supermolecule hydrogel electrolyte film can be effectively regulated and controlled in a large range by adjusting the concentration of the soaked strong electrolyte salt solution, so that the electrolyte film material with excellent repeatable self-healing performance is obtained; however, after further research and tests, the gel electrolyte film prepared by the method has better mechanical properties, but has no better performance on frost resistance, the conductivity of the material is lower under the condition of subzero temperature, the capability of the material to cope with extreme environments is weaker, and the existing hydrogel electrolyte film materials have the defects through testing and comparing the frost resistance of the existing hydrogel electrolyte film materials on the market.
Therefore, there is a need to further explore and improve the preparation method of the hydrogel electrolyte film so as to improve the freezing resistance of the material and meet the use requirements of different application scenes, especially extreme environments.
Disclosure of Invention
The invention aims to provide an antifreeze supramolecular hydrogel electrolyte film and a preparation method and application thereof, wherein the hydrogel electrolyte takes (3- (methylacryloylamino) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt (PDP) and Acrylic Acid (AA) as monomers, and the supramolecular hydrogel with excellent antifreeze performance can be prepared by controlling the ratio of the PDP to water molecules, so that the hydrogel can be used in a low-temperature environment.
The technical scheme disclosed by the invention is as follows: a preparation method of an antifreeze supramolecular hydrogel electrolyte film comprises the steps of firstly weighing (3- (methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt and acrylic acid to be dissolved in deionized water, uniformly stirring to obtain a monomer aqueous solution A, adding an initiator into the monomer aqueous solution A to carry out polymerization reaction to obtain a supramolecular hydrogel, and then soaking the supramolecular hydrogel in a salt solution to finish preparation;
in the monomer aqueous solution A, the molar ratio of (3- (methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt to deionized water was 1: 6.
Further, the molar ratio of the (3- (methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt to the acrylic acid monomer is 1:1 to 1: 8.
Further, the process of stirring to obtain the monomer aqueous solution A is carried out at the rotating speed of 300-800 rpm under the condition of 22-30 ℃, and the stirring is stopped until the uniform and transparent monomer aqueous solution A is obtained.
Further, the polymerization reaction is carried out by: adding an initiator into the monomer aqueous solution A, stirring at a rotating speed of 300-800 rpm at a temperature of 22-30 ℃ until a uniform and transparent solution B is obtained, injecting the solution B into a glass mold, and polymerizing for 6-8 hours at a temperature of 60-65 ℃ to obtain the supramolecular hydrogel material.
Further, the salt solution is one of potassium chloride, lithium chloride, sodium chloride, potassium sulfate, lithium sulfate and sodium sulfate water solutions, and the concentration of the salt solution is 0.5-6M.
The antifreeze supramolecular hydrogel electrolyte film can be obtained by the method, and the film material is a physically crosslinked supramolecular hydrogel which contains a macromolecular chain segment formed by micromolecule polymerization and an electrolyte aqueous solution.
According to the anti-freezing supramolecular hydrogel electrolyte film, a flexible stretchable supercapacitor can be prepared, specifically, a supercapacitor can be prepared by attaching poly 3, 4-ethylenedioxythiophene/polystyrene sulfonate electrodes on two sides of the supramolecular hydrogel electrolyte film, and the conductivity of the supercapacitor can reach 0.12S/m at the temperature of-20 ℃.
Compared with the prior art, the invention has the following advantages:
1. because the PDP contains positively charged N in the zwitterionic material+(CH3)3 And SO with negative charge3 -The group, water molecule can be tightly combined in the charged group of the zwitter-ion material through electrostatic interaction, therefore, the application strictly controls the molar ratio of the monomer PDP to the aqueous solution so that when all water molecules are combined on the polymer chain of the zwitter-ion material through electrostatic interaction in the preparation process, no redundant free water exists in the finished productThe electrolyte film can be frozen below 0 ℃, so that the prepared electrolyte film material has excellent freezing resistance;
2. the method ensures that the prepared hydrogel electrolyte film still has good conductivity in the environment of-20 ℃ by strictly controlling the molar ratio of the monomer PDP to the aqueous solution, and enlarges the application range and application scene of the material;
3. the hydrogel electrolyte film prepared by the invention is a physical cross-linked supermolecule hydrogel, which contains a macromolecular chain segment formed by micromolecule polymerization and an electrolyte aqueous solution, wherein the macromolecular chain segment is obtained by copolymerizing two monomer molecules of (3- (methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt and acrylic acid, a dynamic network is provided by utilizing polyacrylic acid on the basis of ensuring the freezing resistance, the structural integrity and the deformation adaptability of the polyacrylic acid can be ensured by dynamically combining with PDP, and the prepared hydrogel can still maintain 880 percent of fracture strain under the condition of freezing resistance;
4. the amphoteric ion polymer chain segment in the supermolecular hydrogel electrolyte membrane prepared by the invention contains a large number of charged groups, and the charged groups can effectively enhance the interfacial adhesion between the electrode and the gel electrolyte, are beneficial to the bonding of the membrane material and the electrode material to form an effective interface to reduce the interfacial impedance, and can remarkably improve the electrochemical performance of the material.
Drawings
FIG. 1 is a graph of tensile stress strain for the freeze resistant supramolecular hydrogels prepared in examples 1-3;
FIG. 2 is a differential scanning calorimetry test plot of the freeze resistant supramolecular hydrogels prepared in examples 1-3;
FIG. 3 is a graph showing the ionic conductivity of the hydrogel electrolyte prepared in example 4
FIG. 4 is a cyclic voltammogram of the antifreeze flexible supercapacitor prepared in example 4;
FIG. 5 is a constant current charge and discharge curve of the antifreeze flexible supercapacitor prepared in example 4;
FIG. 6 is a graph of the impedance of the freeze resistant flexible supercapacitor made in example 4.
Detailed Description
The technical solution of the present invention is further described below with reference to the accompanying drawings, but not limited thereto, and any modification or equivalent replacement of the technical solution of the present invention without departing from the spirit and scope of the technical solution of the present invention shall be covered by the protection scope of the present invention.
Example 1 preparation of an antifreeze supramolecular hydrogel P (AA-co-PDP) (molar ratio PDP to AA 1:5, molar ratio PDP to water molecules 1: 6)
(1) Weighing 1 g of (3- (methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt and 1.2 mL of acrylic acid solution, dispersing in 0.369 mL of water, adding magnetons, and placing on a magnetic stirrer until a transparent clear solution is formed to obtain a monomer solution;
(2) 0.0094 g of ammonium persulfate is added into the monomer aqueous solution, the monomer solution is injected into a glass mold after being uniformly stirred, and the glass mold is placed on a hot bench (60 ℃/8 h), so that the supermolecule hydrogel can be obtained.
Example 2 preparation of an antifreeze supramolecular hydrogel P (AA-co-PDP) (molar ratio PDP to AA 1:5, molar ratio PDP to water molecules 1: 7)
(1) Weighing 1 g of (3- (methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt and 1.2 mL of acrylic acid solution, dispersing in 0.430 mL of water, adding magnetons, placing on a magnetic stirrer, and stirring until a transparent clear solution is formed to obtain a monomer solution;
(2) 0.0094 g of ammonium persulfate is added into the monomer aqueous solution, the monomer solution is injected into a glass mold after being uniformly stirred, and the glass mold is placed on a hot bench (60 ℃/8 h), so that the supermolecule hydrogel can be obtained.
Example 3 preparation of an antifreeze supramolecular hydrogel P (AA-co-PDP) (molar ratio PDP to AA 1:5, molar ratio PDP to water molecules 1: 8)
(1) Weighing 1 g of (3- (methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt and 1.2 mL of acrylic acid solution, dispersing in 0.492 mL of water, adding magnetons, placing on a magnetic stirrer, and stirring until a transparent clear solution is formed to obtain a monomer solution;
(2) 0.0094 g of ammonium persulfate is added into the monomer aqueous solution, the monomer solution is injected into a glass mold after being uniformly stirred, and the glass mold is placed on a hot bench (60 ℃/8 h), so that the supermolecule hydrogel can be obtained.
Mechanical property test and anti-freezing property test of supermolecular hydrogel
The mechanical property test of the anti-freezing supramolecular hydrogel obtained in the examples 1 to 3 shows that the stress-strain curve of the hydrogel is shown in figure 1, the fracture strain range of the hydrogel is 880% -1180%, the anti-freezing property is shown in figure 2 through the differential scanning calorimetry test, when the molar ratio of PDP to water molecules is 1:6, the water molecules in the hydrogel prepared by the method are just completely and tightly combined by positive and negative charges in polymer chains, so that the hydrogel still has no endothermic peak at-40 ℃, and the hydrogel has excellent anti-freezing property.
Example 4: preparation of anti-freezing supramolecular hydrogel electrolyte P (AA-co-PDP)
The antifreeze supramolecular hydrogel prepared in the example 1 is soaked in a 4M LiCl solution for 24 h to be balanced, and the supramolecular hydrogel electrolyte can be obtained.
Supramolecular hydrogel electrolyte ionic conductivity test
The supramolecular hydrogel electrolyte prepared in example 4 was subjected to an ion conductivity test. The ionic conductivity of the supramolecular hydrogel electrolyte is shown in fig. 3, and the conductivity of the supramolecular hydrogel electrolyte gradually decreases with the decrease of temperature because the decrease of temperature makes the energy barrier for chain-to-chain movement higher, the speed of electron transmission is slower, and the supramolecular hydrogel electrolyte does not have good adhesion with the electrode, thereby the conductivity of the supramolecular hydrogel electrolyte gradually decreases.
Application example, preparation of flexible anti-freezing supercapacitor
And poly (3, 4-ethylenedioxythiophene)/polystyrene sulfonate electrodes are attached to two sides of the supramolecular hydrogel electrolyte film prepared in the embodiment 4, so that the anti-freezing flexible supercapacitor can be prepared.
Electrochemical performance testing of antifreeze flexible supercapacitors
The prepared super capacitor was tested for a circulating current curve, a constant current charge and discharge curve, and an impedance plot, as shown in fig. 4, 5, and 6. The results show that the circulating current curve of the super capacitor at different temperatures keeps a regular rectangle, the scanning rate is 100 mV/s, the constant current charging and discharging curve of the super capacitor at different temperatures keeps a good triangle shape, and the current density during charging and discharging is 0.3 mA/cm2. The impedance of the super capacitor is gradually increased along with the reduction of the temperature, and the super capacitor still has better conductivity of 0.12S/m at the temperature of minus 20 ℃, so that the super capacitor prepared on the basis of the anti-freezing supramolecular hydrogel electrolyte film still keeps better electrochemical performance in a low-temperature environment.
The above description is only an embodiment of the present invention, and not intended to limit the scope of the present invention, and all modifications of equivalent structures and equivalent processes performed by the present specification and drawings, or directly or indirectly applied to other related technical fields, are included in the scope of the present invention.
Claims (7)
1. A preparation method of an antifreeze supramolecular hydrogel electrolyte film comprises the steps of firstly weighing (3- (methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt and acrylic acid to be dissolved in deionized water, uniformly stirring to obtain a monomer aqueous solution A, adding an initiator into the monomer aqueous solution A to carry out polymerization reaction to obtain a supramolecular hydrogel, and then soaking the supramolecular hydrogel in a salt solution to finish preparation;
it is characterized in that the preparation method is characterized in that,
in the monomer aqueous solution A, the molar ratio of (3- (methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt to deionized water was 1: 6.
2. The method for preparing the antifreeze supramolecular hydrogel electrolyte film as claimed in claim 1, wherein the molar ratio of (3- (methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt to acrylic acid monomer is 1: 1-1: 8.
3. The method for preparing the antifreeze supramolecular hydrogel electrolyte film as claimed in claim 1, wherein the stirring process to obtain the monomer aqueous solution A is carried out at a rotating speed of 300-800 rpm under a temperature of 22-30 ℃, and the stirring is stopped until a uniform and transparent monomer aqueous solution A is obtained.
4. The method of preparing a freeze resistant supramolecular hydrogel electrolyte membrane as claimed in claim 1, wherein polymerization is carried out by: adding an initiator into the monomer aqueous solution A, stirring at a rotating speed of 300-800 rpm at a temperature of 22-30 ℃ until a uniform and transparent solution B is obtained, injecting the solution B into a glass mold, and polymerizing for 6-8 hours at a temperature of 60-65 ℃ to obtain the supramolecular hydrogel material.
5. The preparation method of the antifreeze supramolecular hydrogel electrolyte film as claimed in claim 1, wherein the salt solution is one of potassium chloride, lithium chloride, sodium chloride, potassium sulfate, lithium sulfate and sodium sulfate aqueous solution, and the concentration of the salt solution is 0.5-6M.
6. An anti-freeze supramolecular hydrogel electrolyte film, which is characterized in that the film material is prepared by the preparation method of the anti-freeze supramolecular hydrogel electrolyte film according to any one of claims 1 to 5.
7. The application of the antifreeze supramolecular hydrogel electrolyte film in the aspect of supercapacitors, as claimed in claim 6, wherein the supercapacitor can be prepared by attaching poly 3, 4-ethylenedioxythiophene/polystyrene sulfonate electrodes on both sides of the supramolecular hydrogel electrolyte film, and the conductivity of the supercapacitor can reach 0.12S/m at-20 ℃.
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WO2018079592A1 (en) * | 2016-10-27 | 2018-05-03 | リンテック株式会社 | Hydrophilic resin composition and laminated sheet |
CN110265232A (en) * | 2019-06-11 | 2019-09-20 | 南京邮电大学 | A kind of self-healing hydrogel electrolytic thin-membrane and its preparation method and application |
CN111952081A (en) * | 2020-08-25 | 2020-11-17 | 湖北大学 | Preparation method of redox gel electrolyte for all-solid-state supercapacitor |
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WO2018079592A1 (en) * | 2016-10-27 | 2018-05-03 | リンテック株式会社 | Hydrophilic resin composition and laminated sheet |
CN110265232A (en) * | 2019-06-11 | 2019-09-20 | 南京邮电大学 | A kind of self-healing hydrogel electrolytic thin-membrane and its preparation method and application |
CN111952081A (en) * | 2020-08-25 | 2020-11-17 | 湖北大学 | Preparation method of redox gel electrolyte for all-solid-state supercapacitor |
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CN115366510A (en) * | 2022-05-26 | 2022-11-22 | 南京邮电大学 | Artificial bionic skin and application thereof |
WO2023226184A1 (en) * | 2022-05-26 | 2023-11-30 | 南京邮电大学 | Artificial bionic skin and application thereof |
CN115366510B (en) * | 2022-05-26 | 2024-02-23 | 南京邮电大学 | Artificial bionic skin and application thereof |
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